NTN1, netrin 1, 9423

N. diseases: 209; N. variants: 16
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C4748869
Disease: MIRROR MOVEMENTS 4
MIRROR MOVEMENTS 4
disease Disease or Syndrome 1 3 0.400 None 1.000 1 3 2017 2017
CUI: C0038525
Disease: Subarachnoid Hemorrhage
Subarachnoid Hemorrhage
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 501 26 0.350 None 1.000 5 2017 2019
CUI: C0006114
Disease: Cerebral Edema
Cerebral Edema
phenotype Nervous System Diseases Pathologic Function 26 0.300 None 1.000 1 2018 2018
CUI: C0750970
Disease: Cytotoxic Brain Edema
Cytotoxic Brain Edema
phenotype Nervous System Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
CUI: C0525041
Disease: Neurobehavioral Manifestations
Neurobehavioral Manifestations
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Sign or Symptom 77 3 0.300 None 1.000 1 2018 2018
CUI: C0472388
Disease: Cytotoxic Cerebral Edema
Cytotoxic Cerebral Edema
phenotype Nervous System Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
CUI: C0472387
Disease: Vasogenic Cerebral Edema
Vasogenic Cerebral Edema
phenotype Nervous System Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
Subarachnoid Hemorrhage, Spontaneous
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
CUI: C0751530
Disease: Subarachnoid Hemorrhage, Aneurysmal
Subarachnoid Hemorrhage, Aneurysmal
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
Subarachnoid Hemorrhage, Intracranial
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
CUI: C1527311
Disease: Brain Edema
Brain Edema
phenotype Nervous System Diseases Pathologic Function 30 0.300 None 1.000 1 2018 2018
CUI: C0270192
Disease: Perinatal Subarachnoid Hemorrhage
Perinatal Subarachnoid Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
CUI: C0750969
Disease: Vasogenic Brain Edema
Vasogenic Brain Edema
phenotype Nervous System Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Congenital Abnormality 255 282 0.110 None 1.000 5 7 2010 2019
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 2723 2387 0.110 None 1.000 2 1 2009 2009
CUI: C0454455
Disease: Mirror movements disorder
Mirror movements disorder
disease Nervous System Diseases Disease or Syndrome 39 9 0.110 None 1.000 1 2017 2017
CUI: C0027651
Disease: Neoplasms
Neoplasms
group Neoplasms Neoplastic Process 10161 1644 0.100 None 1.000 27 2000 2020
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
group Neoplasms Neoplastic Process 8621 1641 0.100 None 0.950 20 2004 2020
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
group Neoplasms Neoplastic Process 8221 1374 0.100 None 0.938 16 2004 2020
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 6243 355 0.100 None 0.933 15 1997 2018
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 5473 1962 0.100 None 0.929 14 2005 2019
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.100 None 1.000 14 2005 2019
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 2 3 2018 2018
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases Congenital Abnormality 611 158 0.100 None 1.000 2 3 2015 2017
CUI: C0037369
Disease: Smoking
Smoking
phenotype Behavior and Behavior Mechanisms Individual Behavior 391 765 0.100 None 1.000 1 1 2015 2015